Canonical Allele Identifier: CA466526999
Gene: GABBR2 HGNC NCBI

Linked Data

gnomAD v4: 9-98541972-T-C
MyVariant Identifiers: chr9:g.101304254T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98541972T>C , CM000671.2:g.98541972T>C GRCh38
NC_000009.11:g.101304254T>C , CM000671.1:g.101304254T>C GRCh37
NC_000009.10:g.100344075T>C NCBI36
NG_016426.1:g.172226A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000259455.4:c.531A>G MANE Select ENSP00000259455.2:p.Pro177=
ENST00000637410.1:n.309A>G
ENST00000637717.1:c.147A>G ENSP00000490789.1:p.Pro49=
ENST00000259455.3:c.531A>G ENSP00000259455.2:p.Pro177=
ENST00000477471.1:n.318A>G
ENST00000634227.1:n.305A>G
NM_005458.7:c.531A>G NP_005449.5:p.Pro177=
XM_017015331.2:c.237A>G XP_016870820.1:p.Pro79=
NM_005458.8:c.531A>G MANE Select NP_005449.5:p.Pro177=